Canonical Allele Identifier: CA1310652990

Gene: CCDC141

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178856319G= , CM000664.2:g.178856319G=	GRCh38
NC_000002.11:g.179721046G= , CM000664.1:g.179721046G=	GRCh37
NC_000002.10:g.179429291G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443758.7:c.2803C= MANE Select	ENSP00000390190.2:p.Arg935=
ENST00000443758.6:c.2803C=	ENSP00000390190.2:p.Arg935=
ENST00000343876.6:c.1135C=	ENSP00000344627.2:p.Arg379=
ENST00000420890.6:c.2803C=	ENSP00000395995.2:p.Arg935=
ENST00000443758.5:c.2803C=	ENSP00000390190.1:p.Arg935=
NM_173648.3:c.2803C=	NP_775919.3:p.Arg935=
XM_011510991.1:c.2803C=	XP_011509293.1:p.Arg935=
XM_011510992.1:c.2803C=	XP_011509294.1:p.Arg935=
XM_011510993.1:c.2623C=	XP_011509295.1:p.Arg875=
XM_011510994.1:c.859C=	XP_011509296.1:p.Arg287=
XR_923628.1:n.1352+27665G=
XM_011510991.3:c.2803C=	XP_011509293.1:p.Arg935=
XM_011510992.3:c.2803C=	XP_011509294.1:p.Arg935=
XM_011510993.3:c.2623C=	XP_011509295.1:p.Arg875=
XM_017003867.2:c.2803C=	XP_016859356.1:p.Arg935=
XM_017003868.2:c.2803C=	XP_016859357.1:p.Arg935=
XM_017003869.2:c.2803C=	XP_016859358.1:p.Arg935=
XM_017003870.2:c.1513C=	XP_016859359.1:p.Arg505=
XM_017003871.1:c.859C=	XP_016859360.1:p.Arg287=
XR_001738715.2:n.2992C=
NM_173648.4:c.2803C= MANE Select	NP_775919.3:p.Arg935=